Tuesday, September 27, 2011

Day 26- I failed my first exam.

I'm struggling in school more than I thought I would. I studied for hours and I got a 42%. I'm devastated, and I don't know what to do. I contacted the Disability Services office at UI, but I haven't heard back from them yet. 

If anyone has any suggestions on how to (can't find the word... accommodate? no...) deal with it, please help! 

Nothing has changed the past week or so, except that when I spent the weekend with my parents this last weekend, it wiped me out! I slept all day yesterday, and was in quite a bit of pain. Today I'm exhausted and in a lot of pain. 

Still having gastrointestinal issues... :( 

Friday, September 16, 2011

Day 15

It's been a busy couple of days, so I many not remember exactly the symptoms... But--


I've had some neck pain, lower body aches, achey hips, and gastrointestinal issues.


Today I'm really excited to go to a yoga class today-- but I am worried about my energy level.

Tuesday, September 13, 2011

Day 12

I wore myself out yesterday and am really paying for it today. My eyelids feel like there are paper weights on them, and I've got a killer headache. My temper is short, and my patience running thin. I apologize to anyone who encounters me today...

Hoping my completely lazy day makes for a good day tomorrow.

It took me 9 hours to convince myself to inject the B-12. Its not getting easier people. I hate it. I can't seem to make my hand push it in, or let anyone else do it since I know what it will feel like. And the pain isn't even that bad-- I'm just a woos, I guess.

I'm bored out of my mind being stuck in the house all day, but I can't seem to focus on all the schoolwork I have to do. 

Monday, September 12, 2011

Day 11

Yesterday I was in quite a lot of pain, but the burning subsided, THANK GOD! 


Today is a new day, and I feel that I have some energy to get some stuff done!! YAY!!

Saturday, September 10, 2011

NEW SYMPTOM!!!

Today I experienced a new symptom. When we were out in the sun boating, the sun felt extremely hot on me. I haven't been in the sun directly for long periods of time in over a week, so I attributed it to me being a woos. After a while, it began to feel like I had a really bad sunburn and was in the sun. I then went swimming and my face started feeling like I was standing in front of a fire! Even when I put my face in the cold water. When I got back in the boat, it got even worse, and all over my body. I told Eric that it felt like a blow-torch was burning my skin. When we got home, I had Eric look up to see if it was a side effect of any of my medications, but we found that it is a symptom of Lyme. Of course it is... 

Right now its a lot better than it was, but it is still present on my face and the heat makes it a LOT worse!! I couldn't even take dinner out of the oven. :/

Day 9 AND ---> Why I'm not working

So first I need to address something that's really been bothering me. The judgement of not working right now. So let me break it down for you:

In the past 8 years, I have missed way too much work due to being ill. I never knew why I was sick so often but Lyme is hard on your immune system, hence why I got a cold or flu every month or so. I have also had to quit a few jobs because of the symptoms I have experienced such as severe back pain, panic attacks, extreme fatigue, and the list goes on and on. There have been times where I felt I needed to be taken to the emergency room, or just sit in the bathroom for hours because of gastrointestinal issues. 

While I am battling Lyme, I need a lot of sleep. My body is constantly fighting off disease and it needs adequate rest to recoup. I feel embarrassed about this, because it comes of as being lazy, but it just isn't true. A lot of the time I feel like I got run over by a Semi. I know I look fine on the outside... but take a step inside my body and you'll see that it is exhausting being in pain all the time!

Sometimes I am useless, where other times I can actually put makeup on and look nice for my husband :)

Not to mention, I have trouble doing a lot of thinks like cooking, cleaning, talking, walking, shopping, etc. It wears me out!! And sometimes I have what I call a "brain fog". The first time I heard the term brain fog I was in my doctor’s office. The instant I heard that phrase jumped with joy! Because finally, one medical professional, took my symptoms seriously and gave me the words to describe what I was living with day in and day out, a seemingly impenetrable brain fog.  Why was I beginning to stutter?  What was I supposed to do on the days when I could not put two words together? Why did I have to search my mind so hard to find the correct word to use in a sentence? Lyme and Lyme-related co-infections thrive in brain tissue. As they live and multiply, they create infection(s) that in turn cause quite a disturbance in the brain. Infection leads to swelling of tissue. Since the infection begins in the brain, the tissues in the head swell. Swelling in the head causes sinus problems, frightful dreams and painful headaches. (mine include the latter 2). Simply said, the head is supposed to be disease-free and safe-place for the brain. As disease enters the head, the brain can no longer function the way it is designed to function. For example, the brain tries to send signals to cells, however infection makes it impossible for the electric impulse to travel safely to those cells, the cells do not receive the signals they were supposed to receive. A lot of thought is lost in the process.

Anyway-- needless to say, or apparently it is needed-- it is very difficult for me to function in a work setting. I am taking a full load of classes through UI right now, and that seems to be about the most I can do. 

So maybe I look well enough, but I am not exaggerating anything and I know what I need: to stay home and get better.





As for day 9 of treatment... Yesterday I had quite a bit of pain-- sharp pains in my legs that made it difficult to walk. I got another pretty bad headache in the evening which made staying up very exhausting. I'm tired of the shots, and the pills. :( This is all I can muster up for the day... have a good one!

Thursday, September 8, 2011

Day 7

So my pharmacy failed to order the Tindimax last week when I requested it, so I just got it yesterday. I started last night. I got a really really bad headache so I went to bed a little early. Other than that, no problems! Yesterday my other symptoms didn't seem to bother me most of the day. Last night and this morning my pain seemed more frequent than it was yesterday. I had a pretty foggy brain yesterday, but thats been normal. Gastrointestinal issues have subsided, yay! No nausea this morning, yay!

I am now on all of my medications for 2 weeks, then I stop Tindimax for 2 weeks. 

If there is anyone out there, I'll keep you updated!